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Items: 1 to 20 of 271

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949091copy number variation1nstd209human GRCh38 chr20: 31,889,304-31,894,146 , GRCh37.p13 chr20: 30,477,107-30,481,949 TTLL9
    nsv5884153copy number variation1nstd209human GRCh38 chr20: 31,891,933-31,894,332 , GRCh37.p13 chr20: 30,479,736-30,482,135 TTLL9
    nsv5871811copy number variation1nstd209human GRCh38 chr20: 31,891,533-31,895,527 , GRCh37.p13 chr20: 30,479,336-30,483,330 TTLL9
    nsv5871733copy number variation2nstd209human GRCh38 chr20: 31,889,321-31,893,132 , GRCh37.p13 chr20: 30,477,124-30,480,935 TTLL9
    nsv5867739copy number variation2nstd209human GRCh38 chr20: 31,888,693-31,891,132 , GRCh37.p13 chr20: 30,476,496-30,478,935 TTLL9
    nsv5729524mobile element insertion2nstd211human GRCh38 chr20: 31,886,531-31,886,531 , GRCh37.p13 chr20: 30,474,334-30,474,334 TTLL9
    nsv5717906mobile element insertion1nstd211human GRCh38 chr20: 31,892,677-31,892,677 , GRCh37.p13 chr20: 30,480,480-30,480,480 TTLL9
    nsv5714297mobile element insertion1nstd211human GRCh38 chr20: 31,890,154-31,890,154 , GRCh37.p13 chr20: 30,477,957-30,477,957 TTLL9
    nsv5671544insertion1nstd207human GRCh38 chr20: 31,890,201-31,890,201 , GRCh37.p13 chr20: 30,478,004-30,478,004 TTLL9
    nsv5558794mobile element insertion1nstd206human GRCh38 chr20: 31,886,531-31,886,582 , GRCh37.p13 chr20: 30,474,334-30,474,385 TTLL9
    nsv5392217copy number variation2nstd186human GRCh37 chr20: 30,477,107-30,481,988 , GRCh38.p12 chr20: 31,889,304-31,894,185 TTLL9
    nsv5340750translocation1nstd200human GRCh37 chr20: 30,492,161-30,492,161 , GRCh37 chr20: 30,279,679-30,279,679 , GRCh38.p12 chr20: 31,691,876-31,691,876 , GRCh38.p12 chr20: 31,904,358-31,904,358 BCL2L1, TTLL9, 1 more genes
    nsv5327366copy number variation1nstd204human GRCh38.p13 chr20: 31,889,294-31,894,192 , GRCh37.p13 chr20: 30,477,097-30,481,995 TTLL9
    nsv5323109translocation1nstd204human GRCh37.p13 chr20: 30,279,679-30,279,679 , GRCh37.p13 chr20: 30,492,161-30,492,161 , GRCh38.p13 chr20: 31,691,876-31,691,876 , GRCh38.p13 chr20: 31,904,358-31,904,358 BCL2L1, TTLL9, 1 more genes
    nsv5321109copy number variation1nstd204human GRCh38.p13 chr20: 31,924,692-31,924,808 , GRCh37.p13 chr20: 30,512,495-30,512,611 TTLL9
    nsv5300341copy number variation1nstd204human GRCh38.p13 chr20: 31,885,301-31,894,100 , GRCh37.p13 chr20: 30,473,104-30,481,903 TTLL9
    nsv5298850copy number variation1nstd204human GRCh38.p13 chr20: 31,889,321-31,892,732 , GRCh37.p13 chr20: 30,477,124-30,480,535 TTLL9
    nsv5297485copy number variation1nstd204human GRCh38.p13 chr20: 31,902,178-31,904,077 , GRCh37.p13 chr20: 30,489,981-30,491,880 TTLL9
    nsv5288235copy number variation1nstd204human GRCh38.p13 chr20: 31,891,933-31,895,027 , GRCh37.p13 chr20: 30,479,736-30,482,830 TTLL9
    nsv5286961copy number variation1nstd204human GRCh38.p13 chr20: 31,871,729-31,873,944 , GRCh37.p13 chr20: 30,459,532-30,461,747 TTLL9
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